Characterization of the Preferred Stereochemistry for the

Yasumasa Hamada and Takayuki Shioiri ... Kawakami , Kenkichi Noto , Takashi Muto , Yuto Suga , Keiichi Konoki , Mari Yotsu-Yamashita , Makoto Sasaki...
0 downloads 0 Views 282KB Size
Download PDF
J. Nat. Prod. 2004, 67, 559-568

559

Characterization of the Preferred Stereochemistry for the Neuropharmacologic Actions of Antillatoxin W. I. Li,† B. L. Marquez,‡ T. Okino,‡ F. Yokokawa,§ T. Shioiri,§ W. H. Gerwick,*,‡ and T. F. Murray*,† Department of Physiology and Pharmacology, College of Veterinary Medicine, University of Georgia, Athens, Georgia 30602-7389, College of Pharmacy, Oregon State University, Corvallis, Oregon 97331, and Faculty of Pharmaceutical Sciences, Nagoya City University, Nagoya 4678603, Japan Received July 31, 2003

Antillatoxin is a potent ichthyotoxin and cytotoxin previously discovered from the marine cyanobacterium Lyngbya majuscula. Ensuing studies of its mechanism of action showed it to activate the mammalian voltage-gated sodium channel at a pharmacological site that is distinct from any previously described. The structure of antillatoxin, initially formulated from spectroscopic information, was subsequently corrected at one stereocenter (C-4) as a result of synthesis of four different antillatoxin stereoisomers (all possible C-4 and C-5 diastereomers). In the current study these four stereoisomers, (4R,5R)-, (4S,5R)-, (4S,5S)-, and (4R,5S)-antillatoxin, were characterized in five different biological assay systems: ichthyotoxicity to goldfish, microphysiometry using cerebellar granule cells (CGCs), lactose dehydrogenase efflux from CGCs, monitoring of intracellular Ca2+ concentrations in CGCs, and cytotoxicity to Neuro 2a cells. Across these various biological measures there was great consistency in that the natural antillatoxin (the 4R,5R-isomer) was greater than 25-fold more potent than any of the other stereoisomers. Detailed NMR studies provided a number of torsion and distance constraints that were modeled using the MM2* force field to yield predicted solution structures of the four antillatoxin stereoisomers. The macrocycle and side chain of natural (4R,5R)-antillatoxin present an overall “L-shaped” topology with an accumulation of polar substituents on the external surface of the macrocycle and a hydrogen bond between N(H)-7′ and the C(O)-1 carbonyl. The decreased potency of the three non-naturally occurring antillatoxin stereoisomers is certainly a result of their dramatically altered overall molecular topologies. Marine cyanobacteria (blue-green algae) are prolific producers of structurally novel and biologically active natural products and are especially rich in metabolites, which combine amino acid and polyketide portions to form mixed biogenesis metabolites.1 The ranges in biological activity are vast and include anticancer compounds such as curacin A,2 neurotoxins such as kalkitoxin,3 antifungal agents such as hectochlorin,4 and cytotoxins that work by as yet unknown mechanisms such as apratoxin.5 Antillatoxin (ATX) is a structurally novel lipopeptide produced by the pantropical marine cyanobacterium Lyngbya majuscula.6 Blooms of L. majuscula have been associated with adverse effects on human health, including respiratory irritation, eye inflammation, and severe contact dermatitis in exposed individuals. ATX has been reported to be among the most ichthyotoxic metabolites isolated to date from a marine microalga and is exceeded in potency only by the brevetoxins.6 Using cerebellar granule cells, we have shown that ATX produces neuronal death, which is prevented by co-application of an NMDA receptor antagonist.7 This neurotoxic effect of ATX is also antagonized by tetrodotoxin, which suggested an interaction of ATX with voltage-gated sodium channels (VGSC).8 ATX-induced stimulation of Ca2+ influx in cerebellar granule cells was similarly prevented by tetrodotoxin. Additional, more direct, evidence for the VGSC serving as the molecular target for ATX was provided by the demonstration of ATX stimulation of [3H]batrachotoxin binding and 22Na+ influx in cerebellar granule cells.8 Together these results establish ATX as a novel * To whom correspondence should be addressed. (Chemistry) Tel: 541737-5801. Fax: 541-737-3999. E-mail: [email protected]. (Pharmacology) Tel: 706-542-3014. Fax: 706-542-3015. E-mail: Tmurray@ vet.uga.edu. † University of Georgia. ‡ Oregon State University. § Nagoya City University.

10.1021/np0303409 CCC: $27.50

activator of VGSC. The precise recognition site for ATX on the VGSC, however, remains to be defined. The original planar structure of antillatoxin was assembled via standard spectroscopic techniques, while stereochemistry of the two optically active amino acids was accomplished by chiral TLC analysis, revealing an S stereochemistry at both R-carbons. The stereochemistry of C-4 and C-5 was characterized by a combination of homonuclear dipolar and scalar coupling interactions, circular dichroism (CD) spectroscopy, and molecular modeling.6 Interpretation of these spectroscopic data initially indicated that the absolute stereochemistry of antillatoxin was 4S,5R,2′S,5′S. However, spectroscopic data obtained from a synthetic sample of this isomer showed this to be incorrect, and this led to a synthetic project to synthesize all four C-4 and C-5 stereoisomers of antillatoxin, clarifying the natural structure as the (4R,5R)-isomer (Figure 1).9 The objective of the present study was to define the preferred C-4 and C-5 stereochemistry for the pharmacologic actions of ATX in cerebellar granule cells. The role of these two asymmetric carbon atoms in the interaction of ATX with its molecular target was assessed through a pharmacologic characterization of the four ATX isomers. These results indicate that the preferred configuration for ATX-induced alterations in neuronal signaling is presented by the natural (4R,5R)-isomer. Detailed NMR analyses were used to provide numerous distance and torsion angle restraints in the molecular modeling of each of the four tested antillatoxin stereoisomers, thereby leading to an initial characterization of the molecular determinants for antillatoxin interaction with its neuroreceptor target. Results and Discussion Cytotoxicity. We have previously reported that the naturally occurring (-)-ATX produced substantial neuronal death in CGC cultures exposed for 2 h.7,8 This cytotoxic

© 2004 American Chemical Society and American Society of Pharmacognosy Published on Web 02/27/2004

560

Journal of Natural Products, 2004, Vol. 67, No. 4

Li et al.

Figure 1. Four possible stereoisomers about the C-4-C-5 bond of antillatoxin.

Table 1. Biological Evaluation of Antillatoxin Stereoisomers for Ichthyotoxicity, Neurotoxicity, and Extracellular Acidification Rate (microphysiometry) stereoisomer

ichthyotoxicity

microphysiometry

LDH assay

neuro 2a assay

4R,5R 4S,5S 4R,5S 4S,5R

ca. 0.1 µM slight at 10 µM inactive at 10 µM slight at 10 µM

41 nM 5-10 µM 5-10 µM inactive

42 nM 1.4 µM 8.1 µM inactive

0.18 µM 5-10 µM ca. 10 µM ca. 10 µM

Figure 2. Neurotoxic concentration-response profiles of 11-13 days in culture rat cerebellar granule cells exposed 2 h to antillatoxin stereoisomers. Exposure conditions and LDH determination were as described in the Experimental Section. Individual points represent mean - SEM from two separate experiments each performed in triplicate.

response was reflected in elevated LDH efflux into the culture medium. Co-incubation of ATX (100 nM) with tetrodotoxin (1 µM) eliminated ATX neurotoxicity, indicating that VGSCs served as the molecular target for this pharmacologic response.8 The recently synthesized (4S,5R)-, (4R,5R)-, (4S,5S)-, and (4R,5S)-stereoisomers were therefore examined for cytotoxic potency.9 The cytotoxic potencies of the four isomers differed significantly, with the naturally occurring (4R,5R)-configuration being the most potent with a pEC50 value of 7.34 ( 0.01 (45.7 nM). As shown in Figure 2, the (4R,5R)-, (4S,5S)-, and (4R,5S)isomers produced concentration-dependent increases in LDH efflux after 2 h of exposure, whereas neurons treated with the (4S,5R)-isomer were unaffected. The (4R,5R)isomer was 31 and 182 times more potent than the (4S,5S)and (4R,5S)-isomers, respectively (Table 1). In agreement with our previous reports, the cytotoxic response to 100 nM of (4R,5R)-ATX was completely prevented by coincubation with 1 µM tetrodotoxin (data not shown).

Figure 3. Antillatoxin stereoisomer concentration-response profiles for stimulation of extracellular acidification rate in cerebellar granule cells. Neurons were cultured on porous polycarbonate membranes, and acidification rate was monitored by microphysiometry as described in the Experimental Section. Peak acidification rates are expressed as a percentage of basal proton efflux. Individual points represent the mean - SEM from two separate experiments each performed in duplicate.

Natural (4R,5R)-antillatoxin was the most potent of the four isomers to the mouse neuro 2a cell line, with an LD50 ) 0.18 µM. This was 25-50 times more potent than the next most active isomer, (4S,5S)-ATX. The remaining two stereoisomers, (4S,5R)- and (4R,5S)-ATX, were at least 50fold less potent than the natural isomer in this cell line (Table 1). Extracellular Acidification Rate. In an effort to assess the influence of ATX isomers on a functional response of CGCs, extracellular acidification rates of CGCs were evaluated using a Cytosensor microphysiometer. Three of the four ATX isomers tested produced rapid and dramatic increments in the neuronal extracellular acidification rates. The (4R,5R)-isomer was the most potent analogue tested, increasing the extracellular acidification rate by as much as 300% at a concentration of 100 nM (Figure 3). The (4S,5R)-isomer was again inactive, while the (4S,5S)- and (4R,5S)-isomers were active but much less potent than (4R,5R)-ATX. The pEC50 values for these latter three ATX isomers were in remarkable agreement with

Neuropharmacologic Actions of Antillatoxin

Journal of Natural Products, 2004, Vol. 67, No. 4 561

Figure 4. Increases in fluo-3 fluorescence detected by FLIPR in cerebellar granule cells exposed to antillatoxin stereoisomers. Data are from a representative experiment performed in quadruplicate and twice repeated. Basal fluo-3 fluorescence has been subtracted from each value and represented approximately 4000 fluorescence units.

those derived from the cytotoxicity assays. The (4R,5R)isomer was accordingly found to be 135 and 209 times more potent than, respectively, the (4S,5S)- and (4R,5S)-isomers. Ca2+ Influx. We have previously reported that CGCs treated with 100 nM ATX display a rapid increase in cytoplasmic [Ca2+], which is prevented by co-incubation with tetrodotoxin.8 The ATX-induced Ca2+ influx is therefore triggered by activation of VGSC with resultant activation of voltage-gated Ca2+ channels, reversal of the Na+Ca2+ exchanger, and/or relief of the voltage-dependent block of NMDA receptors by Mg2+.8 The configurational preference for the Ca2+ response was therefore explored. As depicted in Figure 4, all four ATX isomers produced concentration- and time-dependent increases in cytoplasmic [Ca2+] as monitored by fluo-3 fluorescence. The stereoselective behavior of the four isomers differed with respect to both potency and efficacy. The (4R,5R)-isomer of ATX was 36 and 89 times more potent than, respectively, the (4S,5S)- and (4R,5S)-isomers (Figure 5). Although concentrations of 1-10 µM of (4S,5R)-ATX produced small, but detectable, increments in cytoplasmic [Ca2+], these data were insufficient to permit calculation of pEC50 values by nonlinear regression analysis with a logistic function. As revealed in Table 1, these stereochemical preferences for stimulation of Ca2+ influx accord favorably with those observed in effects on both cytotoxicity and acidification rate. NMR Studies. Initial structural assignment of 4S,5R stereochemistry to antillatoxin, based on a combination of coupling constants and H-4 to H-5 NOE correlations in the magnitude mode NOESY, was in error.6 The correct 4R,5R stereochemistry of natural antillatoxin was revealed by chemical synthesis of all four stereoisomers at C-4 and C-5.9 Synthetic production of these antillatoxin stereoisomers, in multi-milligram quantities, allowed for a detailed struc-

Figure 5. Antillatoxin stereoisomer concentration-response profiles for stimulation of Ca2+ influx in cerebellar granule cells. Each value is the mean integrated fluo-3 fluorescence response [area under the curve (AUC)] plotted as a function of each stereoisomer concentration.

tural and conformational analysis in addition to the pharmacological studies detailed above. The strategy for the structural analysis of these stereoisomers was to utilize first a suite of contemporary 2D NMR experiments to (a) make firm assignments of all 1H and 13C NMR resonances [1D 1H and 13C NMR, HSQC, and 1H-1H COSY], (b) accurately measure all homonuclear and heteronuclear coupling constants [E-COSY, HSQMBC], and (c) sensitively detect through-space proton-proton interactions without interference from scalar coupling artifacts [T-ROESY]. These data were utilized to provide restraints to a computed three-dimensional energy minimized conformation for each of the four stereoisomers. In the original report of antillatoxin, chiral TLC methods were used to determine an S configuration for two of the four stereocenters in 6 (2′S,5′S). Following synthetic studies that showed natural antillatoxin to be of 4R,5R stereochemistry,9 these two stereocenters were further investigated using additional NMR experiments. Indeed, a de-

562

Journal of Natural Products, 2004, Vol. 67, No. 4

Li et al.

Figure 6. Originally proposed structure of antillatoxin with the incorrectly predicted 4S,5R stereochemistry. Values in bold represent ∆δ values for (4S,5R)-antillatoxin 13C NMR chemical shift - synthetic antillatoxin 13C NMR shift. Values in italics indicate the ∆δ values for (4S,5R)-antillatoxin 1H NMR chemical shift - synthetic antillatoxin 1H NMR shift. Figure 8. (a) Twenty overlaid structures taken from the Monte Carlo search of the constrained energy minimized structure of (4R,5R)antillatoxin. (b) Lowest energy conformation of (4R,5R)-antillatoxin.

Figure 7. DPFGSE 1D NOE spectrum of natural antillatoxin with selective irradiation at H-5. The arrow indicates location of H-4 in the 1H NMR spectrum.

tailed 1H and 13C NMR comparison of the synthetic 4S,5R material and natural antillatoxin revealed significant chemical shift discrepancies clustered around the C-4-C-5 region (Figure 6). Analysis of the original NOESY spectrum for natural antillatoxin revealed that these data were presented as a magnitude calculated spectrum, and thus, the NOE correlation between H-4 and H-5 was likely the result of a COSY (scalar coupling) artifact.6 When H-5 was selectively irradiated using the DPFGSE 1D NOE experiment with a 60 ms Gaussian-shaped pulse,10 only H-7, H-12b, H-13, and H-14 were enhanced (Figure 7). Critically, no enhancement of H-4 was observed, consistent with these protons existing on opposite faces of the macrocycle. With these new NMR data available, the original CD data could be reanalyzed to predict the correct 4R,5R stereochemistry. The solution structure studies of each of the four antillatoxin stereoisomers were initiated with firm assignments of all 1H and 13C NMR resonances. This was accomplished via a combination of 1H NMR, E-COSY,11 and HSQMBC experiments.12 Assignment of the diastereotopic protons at positions C2 and C8′ was achieved through simultaneous interpretation of dipolar couplings and the distance restrained model. In addition, the geminal protons at C-12 (H-12a and H-12b) were assigned on the basis of a combination of ROE data and measurement of 3JCH couplings. With all 1H and 13C NMR resonances assigned, dipolar coupling interactions, homonuclear couplings, and vicinal heteronuclear couplings were analyzed. The TROESY experiment, chosen to reduce strong scalar coupling artifacts that sometimes arise in the standard ROESY experiment, was used to analyze through-space interactions.13 To deduce distance restraints, volumes of all correlations in the T-ROESY spectrum were integrated, normalized, and assigned values of strong (s), medium (m), and weak (w) as follows: s ) 2 ( 1 Å, m ) 2.5 ( 1.5 Å, and w ) 3.0 ( 2 Å. 1H NMR and E-COSY were used to measure 3JHH couplings, and the HSQMBC experiment was

used to measure 3JCH coupling constants. The φ angles of the alanine residue and the diastereotopic protons of glycine were determined through measurement of 3JNH-RH and the formula 3JNH-RH ) 6.7 cos2 θ - 1.3 cos θ + 1.5.14 The φ angle was also calculated through measurement of the 3JHa-CO(i-1) coupling constant and calculating a respective bond angle using the following Karplus equation: 3J 2 15 To determine Ha-CO(i-1) ) 4.0 cos θ - 1.8 cos θ + 0.18. the angle χ of the N-Me valine residue, the 3JHβ-HR and 3J Hβ-CO coupling constants were measured and then used in the formula 3JHβ-HR ) 6.7 cos2 θ - 1.3 cos θ + 1.5 and 3J 2 16 Hβ-CO ) 8.06 cos θ - 0.87 cos θ + 0.47. Molecular Modeling Calculations. Molecular modeling calculations were performed using Macromodel 7.0 utilizing the MM2* force field routine.17 The molecular modeling was initiated by assembling the Dreiding model within Macromodel 7.0 and setting the stereochemistry at each of the four stereocenters. To derive the correct starting bond geometries, a steepest descent (SD) minimization with 100 iterations was performed using the MM2* force field. Distance constraints were entered into a constraint file within the minimization menu, and a 1000 iteration PolakRibier conjugate gradient (PRCG) minimization using the MM2* force field was performed.18 The distance constrained model was then subjected to torsion angle constraints derived from 3JHH homonuclear and 3JCH heteronuclear coupling constants converted to their corresponding angles (calculated with the appropriate Karplus equation). Once all distance and torsion angle constraints were added, an additional PRCG minimization using the MM2* force field was performed. To further probe the available conformations within this minimum, a 1000-step Monte Carlo (MC) search was performed using the MM2* force field. Twenty of the lowest energy structures were overlaid for each of the four isomers and the rms deviations calculated (excluding all hydrogen atoms). For each antillatoxin isomer, the structures with the lowest energy minimum (determined several times throughout the calculation) from the constrained conformational searches are shown in Figures 8-12. (4R,5R)-Antillatoxin ()Natural Antillatoxin). Table 2 tabulates the NMR data used to generate torsion angle and distance constraints for the molecular modeling calculations. A total of 22 distance and nine torsion angle constraints were used in the structure calculation. An error of (20° was tolerated for the torsion angle parameters. The constrained model, using the MM2* force field, had a minimum energy of 258.73 kJ/mol. The MC search generated a new minimum of 255.45 kJ, which was found four

Neuropharmacologic Actions of Antillatoxin

Journal of Natural Products, 2004, Vol. 67, No. 4 563

Figure 9. (a) Twenty overlaid structures taken from the Monte Carlo search of the constrained energy minimized structure (4R,5S)-antillatoxin. (b) Lowest energy conformation of (4R,5S)-antillatoxin.

Figure 10. (a) Twenty overlaid structures taken from the Monte Carlo search of the constrained energy minimized structure (4S,5S)-antillatoxin. (b) Lowest energy conformation of (4S,5S)-antillatoxin.

Figure 11. (a) Twenty overlaid structures taken from the Monte Carlo search of the constrained energy minimized structure (4S,5R)-antillatoxin. (b) Lowest energy conformation of (4S,5R)-antillatoxin.

times (Figure 8b). The 20 lowest energy structures were overlaid (Figure 8a), and an rms deviation was calculated using all non-hydrogen atoms. Of the 20 structures used for the calculation, the energy difference between the minimum and 20th structure was 1.12 kJ/mol. The rms deviation for these structures was 0.57 Å. (4R,5S)-Antillatoxin. Table 3 tabulates the NMR data used to generate torsion angle and distance constraints for the molecular modeling calculations for the (4R,5S)-isomer. A total of 16 distance and seven torsion angle constraints were used in the structure calculation. An error of (20° was tolerated for the torsion angle parameters. The con-

Figure 12. All models are displayed looking down the C-4-C-5 bond axis. (a) Lowest energy conformation of (4R,5R)-antillatoxin. (b) Lowest energy conformation of (4R,5S)-antillatoxin. (c) Lowest energy conformation of (4S,5S)-antillatoxin. (d) Lowest energy conformation of (4S,5R)-antillatoxin.

strained model, using the MM2* force field, had a minimum energy of 284.32 kJ/mol. The MC search generated a new minimum of 259.36 kJ, which was found 16 times (Figure 9b). The 20 lowest energy structures were overlaid (Figure 9a), and an rms deviation was calculated using all non-hydrogen atoms. Of the 20 structures used for the calculation, the energy difference between the minimum and structure 20 was 0.72 kJ/mol. The rms deviation for the 20 isomers was 0.77 Å. (4S,5S)-Antillatoxin. Table 4 tabulates the NMR data used to generate the torsion angle and distance constraints for the molecular modeling calculations for the (4S,5S)isomer. A total of 18 distance constraints and 12 torsion angle constraints were used in the structure calculation. An error of (20° was tolerated for the torsion angle parameters. The constrained model, using the MM2* force field, had a minimum energy of 254.89 kJ/mol. The MC search generated a new minimum of 252.64 kJ, which was found three times (Figure 10b). The 20 lowest energy structures were overlaid (Figure 10a), and an rms deviation was calculated using all non-hydrogen atoms. Of the 20 structures used for the calculation, the energy difference between the minimum and structure 20 was 0.89 kJ/mol. The rms deviation for the 20 isomers was 0.49 Å. (4S,5R)-Antillatoxin. Table 5 tabulates the NMR data used to generate the torsion angle and distance constraints for the molecular modeling calculations for the (4S,5R)isomer. A total of 29 distance constraints and seven torsion angle constraints were used in the structure calculation. An error of (20° was tolerated for the torsion angle

564

Journal of Natural Products, 2004, Vol. 67, No. 4

Li et al.

Table 2. NMR Data for the (4R,5R)-Antillatoxin Isomer (data acquired in DMSO-d6 at 298 K) atom no. 1 2a 2b 3 4 5 6 7 8 9 10 11 12a 12b 13 14 15 16 17 1′ 2′ 3′ 4′ 5′ 6′ 7′ 8′a 8′b 9′ 10′ 11′ 12′ 13′ 14′ 15′

δH 2.73 (d) 3.13 (d) 2.22 (m) 5.07 (d)

3J HH

(Hz)

12.2 12.2 11.1

5.90 (s) 5.28 (s) 1.11 (s) 4.87 (s) 4.91 (s) 0.83 (d) 1.50 (s) 1.78 (s) 1.11 (s) 1.11 (s) 9.24 (d) 5.34 (dq) 4.41 (d) 8.34 (bd) 3.47 (dd) 4.35 (dd)

6.9

8.9 6.5, 8.2 10.9 9.5 1.5, 18.3 9.6, 18.3

HSQMBC (Hz)a

δC 169.8 44.6 146.7 37.6 82.8 129.7 135.6 130.0 140.7 32.1 30.5 111.7 18.3 12.0 17.2 30.5 30.5 42.0 172.6 65.2 167.6 40.2

T-ROESYb

1, 3, 4 (7.0), 12 (5.5) 1, 3, 4 (5.1), 12 (6.1)

2b (s) 2a (s), 4 (m), 13 (m)

2, 3, 5, 6 (4.2), 12, 13 3 (2.5), 4, 6, 7 (4.3), 9′ (